= Clinical programme management - phase I-III
= Protocol and Case Report Form (CRF) design
= Ethics committee and Regulatory agency applications

= Clinical trial monitoring to Good Clinical Practice (GCP), with your =Standard Operating Procedures (SOPs) or ours
= Data management
= Biostatistics. Analysis of pharmacokinetic and pharmacodynamic =relationships, dose-response studies and bioequivalence testing

= Analysis of clinical safety and efficacy data
= Clinical study report writing
= Quality Assurance from an independent, registered Clinical Auditor.